表观遗传学的目标:抑制组蛋白密码的甲基写入。

Current chemical genomics Pub Date : 2011-01-01 Epub Date: 2011-08-22 DOI:10.2174/1875397301005010072
Julianne M Yost, Ilia Korboukh, Feng Liu, Cen Gao, Jian Jin
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引用次数: 0

摘要

越来越多的证据表明,蛋白质赖氨酸甲基转移酶(PKMTs)和蛋白质精氨酸甲基转移酶(PRMTs)与各种人类疾病的发生有关,包括癌症、炎症和精神疾病。鉴于这些蛋白在人类疾病中的重要作用,发现这些酶的选择性小分子抑制剂的努力正迅速获得动力。在本综述中,我们将重点介绍发现选择性 PKMT 和 PRMT 抑制剂的最新进展。此外,我们还展望了开发甲基转移酶抑制剂的未来前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Targets in epigenetics: inhibiting the methyl writers of the histone code.

Targets in epigenetics: inhibiting the methyl writers of the histone code.

Targets in epigenetics: inhibiting the methyl writers of the histone code.

Targets in epigenetics: inhibiting the methyl writers of the histone code.

Growing evidence suggests that protein lysine methyltransferases (PKMTs) and protein arginine methyltransferases (PRMTs) are associated with the development of various human diseases, including cancer, inflammation, and psychiatric disorders. Given the significant role of these proteins in human disease, efforts to discover selective small-molecule inhibitors of these enzymes are quickly gaining momentum. In this review, we focus on the recent progress in the discovery of selective PKMT and PRMT inhibitors. A future perspective on developing methyltransferase inhibitors is also offered.

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